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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393046Generated: October 30, 2026

Pyridine → HCID 53681827, compound

https://huagongshe.com/reaction/2393046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant3-MethylcyclohexanolHCID 11566—
ReactantThiophosphoryl chlorideHCID 19883—
SolventTrichloroethyleneHCID 6575—
ProductHCID 53681827HCID 5368182774.8%

Reaction Steps

A mixture of 3-methylcyclohexanol (5.0 g, 43.8 mmol) in trichloroethylene (300 mL) is added dropwise to a 0°-4° C. mixture of thiophosphoryl chloride (11.13 g, 65.7 mmol) and anhydrous pyridine (5.20 g, 65.7 mmol) in trichloroethylene (125 mL) over a 1 hour period under a nitrogen atmosphere. The resultant reaction mixture is stirred at 0°-4° C. for 1 hour and is then warmed to room temperature and stirred at room temperature for 8 hours. A white solid gradually precipitates. The white solid is filtered from the reaction mixture. The resultant reaction mixture is concentrated in vacuo to a residue. Successive aliquots of toluene (100 mL) are added to the residue and then separately are evaporated in vacuo to give 7.57 g (70%) of (3-methylcyclohexyl)-thiophosphoryl dichloride which can be used directly without further purification as the starting material for Example 23.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05804569
Source datasetuspto-grants-1998_09
ORD IDord-56d43a3b272a4c4cad885821ea0cf8c7
Source noteuspto-grants-1998_09